Khan AT - Search Results

1

Regioselective synthetic approach for key precursors of 6-arylbenzo[c]phenanthridin-10-ol derivatives: a useful compound for selective chromogenic recognition of fluoride.

Yashmin S, Mondal S, Das R, Banerjee P, Khan AT. Yashmin S, et al. Among authors: khan at. Org Biomol Chem. 2022 Sep 21;20(36):7302-7315. doi: 10.1039/d2ob01260j. Org Biomol Chem. 2022. PMID: 36069360

2

K₂CO₃ catalyzed regioselective synthesis of thieno[2,3-b]thiochromen-4-one oximes: access to the corresponding amine and nitroso derivatives.

Mahato K, Bagdi PR, Khan AT. Mahato K, et al. Among authors: khan at. Org Biomol Chem. 2017 Jul 5;15(26):5625-5634. doi: 10.1039/c7ob01033h. Org Biomol Chem. 2017. PMID: 28640318

3

Camphorsulfonic Acid Catalyzed One-Pot Three-Component Reaction for the Synthesis of Fused Quinoline and Benzoquinoline Derivatives.

Gattu R, Bagdi PR, Basha RS, Khan AT. Gattu R, et al. Among authors: khan at. J Org Chem. 2017 Dec 1;82(23):12416-12429. doi: 10.1021/acs.joc.7b02159. Epub 2017 Nov 7. J Org Chem. 2017. PMID: 29052992

4

Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles.

Gattu R, Bhattacharjee S, Mahato K, Khan AT. Gattu R, et al. Among authors: khan at. Org Biomol Chem. 2018 May 23;16(20):3760-3770. doi: 10.1039/c8ob00736e. Org Biomol Chem. 2018. PMID: 29722779

5

Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes.

Gattu R, Mondal S, Ali S, Khan AT. Gattu R, et al. Among authors: khan at. Org Biomol Chem. 2019 Jan 2;17(2):347-353. doi: 10.1039/c8ob02333f. Org Biomol Chem. 2019. PMID: 30548050

6

Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth(iii) triflate: an easy access to 2,3-dialkylquinolines.

Ali S, Gattu R, Singh V, Mondal S, Khan AT, Dubey G, Bharatam PV. Ali S, et al. Among authors: khan at. Org Biomol Chem. 2020 Mar 4;18(9):1785-1793. doi: 10.1039/c9ob02214g. Org Biomol Chem. 2020. PMID: 32073090

7

Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity.

Mondal S, Mahato K, Arora N, Kankane D, Singh UP, Ali S, Khan AH, Ghosh SS, Khan AT. Mondal S, et al. Among authors: khan ah, khan at. Org Biomol Chem. 2020 Jun 7;18(21):4104-4113. doi: 10.1039/d0ob00054j. Epub 2020 May 20. Org Biomol Chem. 2020. PMID: 32432294

8

Copper(ii) triflate catalyzed three-component reaction for the synthesis of 2,3-diarylquinoline derivatives using aryl amines, aryl aldehydes and styrene oxides.

Ali S , Khan AT . Ali S , et al. Among authors: khan at. Org Biomol Chem. 2021 Apr 14;19(14):3255-3262. doi: 10.1039/d1ob00125f. Epub 2021 Mar 25. Org Biomol Chem. 2021. PMID: 33885580

9

Synthesis of biologically active fused 1,4-oxathiin derivatives from 4-hydroxydithiocoumarins, arylacetylenes and dimethyl sulfoxide by Cu(i)-catalyzed C-H functionalization and cross-dehydrogenative C-S coupling reactions.

Mondal S, Yashmin S, Ali R, Soundaram R, Ghosh SS, Khan AT. Mondal S, et al. Among authors: khan at. Org Biomol Chem. 2021 Jul 14;19(26):5818-5826. doi: 10.1039/d1ob00846c. Epub 2021 Jun 11. Org Biomol Chem. 2021. PMID: 34113949

10

Metal-free synthesis of quinoline-2,4-dicarboxylate derivatives using aryl amines and acetylenedicarboxylates through a pseudo three-component reaction.

Ali S, Khan AT. Ali S, et al. Among authors: khan at. Org Biomol Chem. 2021 Aug 28;19(32):7041-7050. doi: 10.1039/d1ob01188j. Epub 2021 Aug 3. Org Biomol Chem. 2021. PMID: 34341812

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